Choline Acetyltransferase anticorps (AA 131-704)

N° du produit ABIN7870510

Cet anticorps anti-Choline Acetyltransferase Polyclonal Lapin (ABIN7870510) détecte spécifiquement Choline Acetyltransferase dans WB, ELISA et FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour Choline Acetyltransferase anticorps (AA 131-704) (ABIN7870510)

Antigène: Choline Acetyltransferase (CHAT) (Choline O-Acetyltransferase (CHAT))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Choline Acetyltransferase est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Détail du produit anti-Choline Acetyltransferase anticorps

Épitope: AA 131-704

Fonction: Choline Acetyltransferase Antibody / ChAT

Purification: Antigen affinity purified

Immunogène: Recombinant human protein (amino acids L131-S704) was used as the immunogen for the Choline Acetyltransferase antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Choline Acetyltransferase antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the Choline Acetyltransferase antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur Choline Acetyltransferase

Antigène: Choline Acetyltransferase (CHAT) (Choline O-Acetyltransferase (CHAT))

Autre désignation: Choline Acetyltransferase

Sujet: Choline acetyltransferase (commonly abbreviated as ChAT, but sometimes CAT) is a transferase enzyme responsible for the synthesis of the neurotransmitter acetylcholine. In humans, the choline acetyltransferase enzyme is encoded by the CHAT gene. This gene product is a characteristic feature of cholinergic neurons, and changes in these neurons may explain some of the symptoms of Alzheimer's disease. Polymorphisms in this gene have been associated with Alzheimer's disease and mild cognitive impairment. Mutations in this gene are associated with congenital myasthenic syndrome associated with episodic apnea. Multiple transcript variants encoding different isoforms have been found for this gene, and some of these variants have been shown to encode more than one isoform.

UniProt: P28329

Pathways: Skeletal Muscle Fiber Development